In February 2008 our lives took a turn in a different direction when our daughter Emily was diagnosed at 18 months, with a rare chromosome disorder called Chromosome 17q21.31 Microdeletion Syndrome. Now called Koolen-deVries Syndrome. We decided to share our daughter Emily’s story here at Emily Ann's Kloset, so that other parents out there, would have something to read & inspire them when they sat down to Google their child’s new diagnosis. We hope you enjoy taking a look around our little corner of the web.
peppermint bark
I have a feeling that May is going to be …
jelly roll check quilt: a short cut quilt series
Oh hello there and happy Monday! It’s no secret I …
AGF Stitched Quilt: Filigree!
Happy Monday! It’s time for another fun AGF Stitched project …
happy birthday emily ann
It was a day filled with giggles, happy smiles, BBQing …
two peas in a pod
Life is filled with many uncertainties for this sweet girl …
about a quilt
Earlier in the year, I started to browse through fabrics …
